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Peng Fan

Showing results (281-290 of 332) with videos related to

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Clinical and Experimental Hypertension (New York, N.Y. : 1993)|July 19, 2017
Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndromeKun-Qi Yang, Chao-Xia Lu, Peng Fan, et al.
Environmental Science & Technology|April 15, 2011
Effects of cake collapse caused by deposition of fractal aggregates on pressure drop during ceramic filtrationWei Zhang, Cai-Ting Li, Xian-Xun Wei, et al.
Nature Biotechnology|December 17, 2013
Genome-wide localization of small moleculesLars Anders, Matthew G Guenther, Jun Qi, et al.
Frontiers in Pediatrics|July 18, 2022
Corrigendum: Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese FamilyDi Zhang, Yi Qu, Xue-Qi Dong, et al.
Cell Stem Cell|December 22, 2015
3D Chromosome Regulatory Landscape of Human Pluripotent CellsXiong Ji, Daniel B Dadon, Benjamin E Powell, et al.
ACS Nano|April 14, 2017
Broken Symmetry Induced Strong Nonlinear Optical Effects in Spiral WS<sub>2</sub> NanosheetsXiaopeng Fan, Ying Jiang, Xiujuan Zhuang, et al.
Reviews in Cardiovascular Medicine|July 30, 2024
De-Escalation Dual Antiplatelet Therapy Prevail over Potent P2Y12 Inhibitor Monotherapy in Patients with Acute Coronary Syndrome Undergone Percutaneous Coronary Intervention: A Network Meta-AnalysisJing-Wen Ding, Yang Chen, Zuo-Zhong Yu, et al.
Nano Letters|April 3, 2020
Wavelength-Tunable Interlayer Exciton Emission at the Near-Infrared Region in van der Waals Semiconductor HeterostructuresLihui Li, Weihao Zheng, Chao Ma, et al.
American Journal of Hypertension|April 13, 2019
A Novel Frameshift Mutation of SCNN1G Causing Liddle Syndrome with NormokalemiaPeng Fan, Yu-Mo Zhao, Di Zhang, et al.
BMJ Oncology|January 31, 2025
Baseline tumour vessel perfusion as a non-invasive predictive biomarker for immune checkpoint therapy in non-small-cell lung cancerZhenhua Liu, Ke Ma, Qingzhu Jia, et al.
Pageof 34

Showing results (281-290 of 332) with videos related to

Sort By:
Pageof 34
Clinical and Experimental Hypertension (New York, N.Y. : 1993)|July 19, 2017
Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndromeKun-Qi Yang, Chao-Xia Lu, Peng Fan, et al.
Environmental Science & Technology|April 15, 2011
Effects of cake collapse caused by deposition of fractal aggregates on pressure drop during ceramic filtrationWei Zhang, Cai-Ting Li, Xian-Xun Wei, et al.
Nature Biotechnology|December 17, 2013
Genome-wide localization of small moleculesLars Anders, Matthew G Guenther, Jun Qi, et al.
Frontiers in Pediatrics|July 18, 2022
Corrigendum: Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese FamilyDi Zhang, Yi Qu, Xue-Qi Dong, et al.
Cell Stem Cell|December 22, 2015
3D Chromosome Regulatory Landscape of Human Pluripotent CellsXiong Ji, Daniel B Dadon, Benjamin E Powell, et al.
ACS Nano|April 14, 2017
Broken Symmetry Induced Strong Nonlinear Optical Effects in Spiral WS<sub>2</sub> NanosheetsXiaopeng Fan, Ying Jiang, Xiujuan Zhuang, et al.
Reviews in Cardiovascular Medicine|July 30, 2024
De-Escalation Dual Antiplatelet Therapy Prevail over Potent P2Y12 Inhibitor Monotherapy in Patients with Acute Coronary Syndrome Undergone Percutaneous Coronary Intervention: A Network Meta-AnalysisJing-Wen Ding, Yang Chen, Zuo-Zhong Yu, et al.
Nano Letters|April 3, 2020
Wavelength-Tunable Interlayer Exciton Emission at the Near-Infrared Region in van der Waals Semiconductor HeterostructuresLihui Li, Weihao Zheng, Chao Ma, et al.
American Journal of Hypertension|April 13, 2019
A Novel Frameshift Mutation of SCNN1G Causing Liddle Syndrome with NormokalemiaPeng Fan, Yu-Mo Zhao, Di Zhang, et al.
BMJ Oncology|January 31, 2025
Baseline tumour vessel perfusion as a non-invasive predictive biomarker for immune checkpoint therapy in non-small-cell lung cancerZhenhua Liu, Ke Ma, Qingzhu Jia, et al.
Pageof 34